US1571074A - Recovered inorganic filter aid and process of producing the same - Google Patents
Recovered inorganic filter aid and process of producing the same Download PDFInfo
- Publication number
- US1571074A US1571074A US614707A US61470723A US1571074A US 1571074 A US1571074 A US 1571074A US 614707 A US614707 A US 614707A US 61470723 A US61470723 A US 61470723A US 1571074 A US1571074 A US 1571074A
- Authority
- US
- United States
- Prior art keywords
- diatomaceous earth
- filter
- filtration
- sugar
- aid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 40
- 239000005909 Kieselgur Substances 0.000 description 31
- 238000001914 filtration Methods 0.000 description 20
- 238000001354 calcination Methods 0.000 description 15
- 150000003839 salts Chemical class 0.000 description 13
- 238000001035 drying Methods 0.000 description 10
- 239000012065 filter cake Substances 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 239000012535 impurity Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 238000000227 grinding Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 230000004927 fusion Effects 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 241000206761 Bacillariophyta Species 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 150000003841 chloride salts Chemical class 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- -1 for example Chemical compound 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/10—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate
- B01J20/14—Diatomaceous earth
Definitions
- UNITED STATES may s. rnarcnnn, or os anonnns, camnonma, assrenonfnx MESNE as- SIGNMENTS, TO THE OELITE COMPANY, A CORPORATION OF DELAWARE.
- wet diatomaceous earth for example, is calcined, hard lumps are formed.
- colloidal silica present in the wet diatomaceous earth acts as a high temperature bond.
- bonding action has been Application filed January 24, 1928. Serial No. 614,707.
- a second difiiculty which has been experienced in previous attempts to recover the diatomaceous earth for reuse in filtering sugar'solutions is the presence of inorganic salts in the recovered diatomaceous earth due to accumulation of such salts in the press cake during filtration.
- I calcine at temperatures just sufficient to burn out the organic material, I calcine at temperatures sufficiently high to remove, by volatilization, or by combining with the silica, a lar e part of the in organic impurities also.
- sodium chloride and potassium chloride for example,'begin to volatilize at temperatures as low as 1700 F.
- I may use a rotary calciner in which the diatomaceous earth to be recovered is heated by an internal oil, coal or gas fire, or I may use any other of the numerous types of calciners or roasters in commercial use.
- I have "iven as the preferred temperature, 1800 Temperatures up to 2400 F. are not objectionable as long as the filtration accelerator being recovered does not fuse 01' clinker together at such temperature.
- a lower temperature than 1800 F. may be used, although the efiiciency of the accelerator and the extent of purification from inorganic impurities decreases .as the temperature'is lowered appreciably below 1800 F.
- the salt may be incorporated with the material in solution, or in finely divided form, before calcination of the mixture. As the mixture of salt and diatomaceous earth is heated, the salt first melts into the pores of the diatomaceous earth, later it vaporizes as proven by analysis of the original and of the calcined mixture. The vapor escaping from the pores of the kieselguhr may open wider such pores.
- the hot vapor in contact with the diatomaceous earth promotes fusion and in such a partial fusion, the fine particles of clay and the finest particles of the silica will fuse prior to the fusion of the larger diatom skeletons.
- the salt changes or destroys a considerable part of the fine dust or clay which retards filtration of liquors throu h the earth.
- meta lic salts or compounds may be used in place of the sodium chloride, for example, calcium chloride, magnesium chloride, or any chloride or halide of any alkali metal or alkaline earth metal, or'
- salts which produce the desired result, namely, an increase in the efliciency of the product as a filter-aid, and any of such salts may be used either singly or in combination.
- a material adapted for use in fi tration consisting of an inorganic filter-aid produced by first drying, then finely dividing, and then finally calcmin filter cake result ing from filtering operatihns and containing such filter aid to remove part of the inor-' ganic impurities therefrom.
- a material adapted for use as a filteraid which consists of diatomaceous earth obtained by dryin then finely dividing, and then calcining lter cake resulting from filtermg operations and containing such diatomaceous earth to remove part of the inorganic impurities therefrom.
- a new article of commerce consistin of diatomaceous earth derived from spent ter ress residue containin such earth; by first rylng such residue, t en reducing it to a conditlon of fine division; and finally calcining the finely divided dried residue by subjecting it to a temperature of approximately 1800 F.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Inorganic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Silicon Compounds (AREA)
Description
. Patented Jan. 26, 1926.
UNITED STATES may s. rnarcnnn, or os anonnns, camnonma, assrenonfnx MESNE as- SIGNMENTS, TO THE OELITE COMPANY, A CORPORATION OF DELAWARE.
RECOVERED INORGANIC FILTER AID AND PROCESS OF PRODUCING THE BAH].
1| Drawing.
To all whom it may concern:
Be it known that I, HARRY S. THATGHER,
' a citizen of the United States, residing at tion is widespread. In the sugar industry,
for example, it is the custom to mix raw sugar, diatomaceous earth and water in the proportions of two thousand pounds sugar, about seven pounds diatomaceous earth and thirteen hundred pounds of water. When the solution of the sugar is complete the liquor is pumped through a pressure filter. Here the diatomaceous earth is collected,
' with suspended matter originally present in the sugar, to give a more or less pervious filter cake. When the cake has become so thick that the rate of filtration is very slow, the press is drained; the filter cake is removed from the press and treated with water toremove as much as possible of the sugar contained in the filter cake; the diatomaceous earth, now nearly free of sugar, is discarded.
Many attempts have been made to recover, for reuse, this diatomaceous earth or other aid used in the filtration. Usually, the recovery process has consisted essentially in calcining the used filter-aid, such as diatomaceous earth, to carbonize or burn oflf entirely the organic impurities. Such attempts have not been successful as evidenced by the fact that many manufacturers have abandoned equipment once installed for recovery purposes.
I have discovered the reason for some of the difliculty which these previous investigators have experienced, and I have found also simple but effective means of overcoming the difliculty.
When wet diatomaceous earth, for example, is calcined, hard lumps are formed.
The colloidal silica present in the wet diatomaceous earth acts as a high temperature bond. When such bonding action has been Application filed January 24, 1928. Serial No. 614,707.
produced, it is impracticable later to dislntegrate the hard lumps into individual diatoms, and it is the diatom skeleton which is important in accelerating filtration.-
able extent and then disintegrated of reduced by grinding or millin to a condition of powder or fine division, or example, approximately to individual diatoms, and is then calcined at a suitable temperature, preferably at about 1800 F. The preliminary drying and the reduction to a condition of fine division are both important in producing a material of the desired efiiciency as a filtration accelerator or filter-aid. The pre drying facilitates the. grinding and it is llkely that it dehydrates or destroys much of the colloidal silica or silicic acid present in the filter cake. Whatever the changes actually produced by the drying and grinding previous to calcining, I have found that such pre-drying and pre-grinding have an advantageous effect as illustrated in the fol lowing example of. the application of my new process: A sample of diatomaceous earth which had been 'used in filtering raw Hawaiian sugar at a San Francisco refinery was heated in a mufiie furnace up to 1800 F., at which temperature it was maintained for one hour. the'muflle was then ground as thoroughly as possible in a Williams swing hammer mill. A test of it was then made to determine its efliciency as a filtration accelerator. It was mixed with 60 Brix raw sugar solution in the proportion of sixteen pounds for each 3300 pounds of sugar solution. The
temperature was maintained at C. and
the mixture forced through a pressure filter, the pressure on the solution being varied from ten pounds at the start to forty pounds, according to a regular schedule. .In one half hour there was filtered 3.7 gallons of filtrate, calculated for each square foot of filtering area. The procedure was now re- The material removed from' peated with the important exception that the diatomaceous earth fromthesugar refinery was first thoroughly dried at 284 F. and then milled in the Williams swing hammer mill previous to calcining. As before, the temperature in the mufiie was raised to 1800 F., and maintained at that point for one hour. The proportion of recovered diatomaceous earth to sugar, the temperature of filtration, the schedule of pressure in creases during the filtration test, and all other conditions with the single exception noted above, were maintained the same. In this case, however, I obtained a rate of filtration which was 179% that obtained with the diatomaceous earth which had not been disintegrated after drying and previous to calcining. In other words, I obtained in this experiment 6.65 gallons filtrate per square foot of filter area, during a thirty minute filtration test. It is a remarkable fact that the used diatomaceous earth filtercake,-dried and ground before 'calcination, showed a higher filtration rate than the fresh diatomaceous earth originally used as a filter-aid from which the filter-cake was formed that was used in making the recovered filter-aid.
A second difiiculty which has been experienced in previous attempts to recover the diatomaceous earth for reuse in filtering sugar'solutions is the presence of inorganic salts in the recovered diatomaceous earth due to accumulation of such salts in the press cake during filtration. Instead of calcining, in my process, at temperatures just sufficient to burn out the organic material, I calcine at temperatures sufficiently high to remove, by volatilization, or by combining with the silica, a lar e part of the in organic impurities also. It is well known that sodium chloride and potassium chloride, for example,'begin to volatilize at temperatures as low as 1700 F. This rate of 'volatilization is increased in the presence of diatomaceous earth, which absorbs the melted chlorides in its highly porous structure and thereby exposes exceptionally large surfaces from which the hot chlorides may evaporate. Further, the calcium salts which are-found in sugar press cake are first decomposed by high temperatures, such as I use, and then combined with the silica, of which diatomaceous earth is chiefly composed, to give insoluble calcium silicate, for example. To illustrate the above point, we have the following typical data; a sample of diatomaceous earth used in the filter press of 'a sugar refinery was found to contain 0.93 pounds of soluble inorganic materials (ash after ignition of recovered product on evaporation of a ueous extract) for each one hundred poun s of dried filter cake. By heating this dried filter cake to the preferred temperature, 1800 F. I have actually reduced this amount of water soluble inorganic material to less than one-third what it was originally, that is, to 0.28 pounds.
' The sugar industry especially is not able to use diatomaceous earth containing large quantities of soluble inorganic impurities. It has been found that each pound of inorganic material introduced into the sugar refiners liquors, increases the non-crystallizable su ar in the molasses by five pounds.
While I have referred to the use of a mufiie furnace, I may use a rotary calciner in which the diatomaceous earth to be recovered is heated by an internal oil, coal or gas fire, or I may use any other of the numerous types of calciners or roasters in commercial use. I have "iven as the preferred temperature, 1800 Temperatures up to 2400 F. are not objectionable as long as the filtration accelerator being recovered does not fuse 01' clinker together at such temperature. A lower temperature than 1800 F. may be used, although the efiiciency of the accelerator and the extent of purification from inorganic impurities decreases .as the temperature'is lowered appreciably below 1800 F.
I have found that the incorporation of such chemicals as sodium chloride aids also in improving the filtration efliciency of the recovered diatomaceous earth, the reason being presumably that it increases the purity and the structural change of the particles and eliminates soluble salts. The salt may be incorporated with the material in solution, or in finely divided form, before calcination of the mixture. As the mixture of salt and diatomaceous earth is heated, the salt first melts into the pores of the diatomaceous earth, later it vaporizes as proven by analysis of the original and of the calcined mixture. The vapor escaping from the pores of the kieselguhr may open wider such pores. Also, the hot vapor in contact with the diatomaceous earth promotes fusion and in such a partial fusion, the fine particles of clay and the finest particles of the silica will fuse prior to the fusion of the larger diatom skeletons. In other words, the salt changes or destroys a considerable part of the fine dust or clay which retards filtration of liquors throu h the earth.
Various other meta lic salts or compounds may be used in place of the sodium chloride, for example, calcium chloride, magnesium chloride, or any chloride or halide of any alkali metal or alkaline earth metal, or'
other salts, which produce the desired result, namely, an increase in the efliciency of the product as a filter-aid, and any of such salts may be used either singly or in combination.
In carrying out the process with the addition of sodium chloride or other salts, the
several steps of pre-drying, grinding and milling to a pulverized c ndition and calcination at a temperature of about 1800 F. (or at least above 1500 F.) are follownl as above described the salt being added previous to the calcination, for example, during the grindin operation.
- What I c aim is:
1. The process of recovering an inorganic filter-aid after use in filtration which consists in drying the filter-cake containing such filter-aid, then finely dividing it, and then calcining the disintegrated material at a tem erature sutficiently high to remove part of t e inorganic impurities.
2. The process of recovering diatomaceous earth after use in filtration which consists in drying the filter press cake containing such diatomaceous earth, then finely dividing it and then calcining the disintegrated material to reduce the amount of inorganic impurities.
3. The process as set forth in claim 2, the calcination being carried out in the presence of an added salt of an alkali-formin metal.
4. A material adapted for use in fi tration consisting of an inorganic filter-aid produced by first drying, then finely dividing, and then finally calcmin filter cake result ing from filtering operatihns and containing such filter aid to remove part of the inor-' ganic impurities therefrom.
5. A material adapted for use as a filteraid which consists of diatomaceous earth obtained by dryin then finely dividing, and then calcining lter cake resulting from filtermg operations and containing such diatomaceous earth to remove part of the inorganic impurities therefrom.
6. The herein described rocess of recovering diatomaceous earth rom spent filter press residue containing such earth; said process consisting in first drying such residue, then reducin the dried residue to a condition of fine division; and finally calcining the finely divided dried residue by subjecting it to a temperature of ap roximately 1800 F. to produce an e ective filter aid.
7. A new article of commerce consistin of diatomaceous earth derived from spent ter ress residue containin such earth; by first rylng such residue, t en reducing it to a conditlon of fine division; and finally calcining the finely divided dried residue by subjecting it to a temperature of approximately 1800 F.
In testimony whereof I have hereunto subsigiged my name this 19thday of January u nar s. 'rnarcrma.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US614707A US1571074A (en) | 1923-01-24 | 1923-01-24 | Recovered inorganic filter aid and process of producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US614707A US1571074A (en) | 1923-01-24 | 1923-01-24 | Recovered inorganic filter aid and process of producing the same |
Publications (1)
Publication Number | Publication Date |
---|---|
US1571074A true US1571074A (en) | 1926-01-26 |
Family
ID=24462388
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US614707A Expired - Lifetime US1571074A (en) | 1923-01-24 | 1923-01-24 | Recovered inorganic filter aid and process of producing the same |
Country Status (1)
Country | Link |
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US (1) | US1571074A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2493381A (en) * | 1947-07-01 | 1950-01-03 | Us Finishing Company | Process for crease-proofing textiles |
US5938927A (en) * | 1996-09-30 | 1999-08-17 | Aluminum Company Of America | Process for extracting oil from contaminated filter media |
-
1923
- 1923-01-24 US US614707A patent/US1571074A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2493381A (en) * | 1947-07-01 | 1950-01-03 | Us Finishing Company | Process for crease-proofing textiles |
US5938927A (en) * | 1996-09-30 | 1999-08-17 | Aluminum Company Of America | Process for extracting oil from contaminated filter media |
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